9-Bromo-10-(phenyl-d5)anthracene CAS 1185864-38-3

9-Bromo-10-(phenyl-d5)anthracene CAS 1185864-38-3 Deuterium (D or 2H) is a stable non radioactive isotope of hydrogen, also known as hydrogen. There is a proton and a neutron in the deuterium nucleus, and its relative atomic weight is twice that of ordinary hydrogen. There is 0.02% deuterium in the game vegetable, and the content in nature is about one thousandth of the general hydrogen.

Good News, For the category of OLED Terminal compounds, our in stock information below:

In biomedical related fields, hydrogen atoms at some sites in the drug molecule are replaced by its stable isotope deuterium, that is, the drug is labeled with hydrogen, and then combined with liquid mass spectrometry to quickly obtain and analyze data, which makes this technology widely used in the study of the absorption, distribution, metabolism and excretion of drugs in vivo.

For example, in drug metabolism, use non labeled and deuterium labeled drug mixtures to analyze and detect metabolites through GC. MS or LC. MS, and determine the structure of metabolites. The deuterium labeling of drugs can not only facilitate the localization and analysis of metabolites in vivo, but also help to find new metabolites for the study of metabolic mechanism. Deuterium labeled drugs were used for clinical metabolic kinetics study. It has the following advantages: high sensitivity and precision, fast and convenient testing, and high data reliability.

As an intermediate in organic synthesis

 

Fluorescent molecular dyes: Fluorescent molecular dyes have a wide range of applications in biological labeling, optical sensing, imaging technology, and other fields. The tritium derivative of this compound, due to its unique polyaromatic ring structure, may endow the dye with special optical properties. It can be used as a precursor for the synthesis of fluorescent dyes, and dye molecules with specific fluorescent properties can be prepared through functional group conversion and further chemical modification. These dye molecules can emit strong fluorescent signals inside living organisms or on material surfaces for tracking, detection, and imaging.

As an intermediate in organic synthesis

 

Organic luminescent materials: They play an important role in display technology, lighting technology, and other fields. The tritium derivatives of this compound have potential luminescent properties and can be used as luminescent layers or dopants for devices such as organic light-emitting diodes (OLEDs). It can prepare OLED materials with efficient and stable luminescent properties by optimizing synthesis conditions and subsequent processing techniques. These materials have broad application prospects in fields such as display screens and lighting fixtures, which can improve display effects and lighting efficiency.
Synthesis of other organic compounds: The tritium derivatives of this compound, as organic synthesis intermediates, have rich reactivity and functional group conversion potential. They can be converted into other useful chemical structures through various chemical methods such as substitution reactions, addition reactions, coupling reactions, etc. These transformation products have wide application value in fields such as drug synthesis, pesticide preparation, and functional material development.

As a pharmaceutical intermediate

 

In the field of medicine, this compound can serve as an important synthetic block or intermediate. Its unique chemical structure and functional groups enable it to be transformed into compounds with pharmacological activity through a series of chemical reactions. These compounds may have various biological activities such as anti-inflammatory, anti-tumor, and antibacterial, providing strong support for the development of new drugs. The bromine atoms and tritium substituted phenyl groups in this substance provide abundant functional group conversion potential. Through chemical methods such as substitution reactions, addition reactions, and coupling reactions, bromine atoms can be converted into other functional groups such as hydroxyl, amino, carboxyl, etc., thereby further synthesizing drug molecules with specific pharmacological activities. Introducing tritium substituted phenyl groups during synthesis may help improve the stability and bioavailability of drugs.

As a pharmaceutical intermediate

 

The special properties of tritium substituted phenyl groups may make drug molecules more stable in the body, less easily metabolized or degraded, thereby prolonging the duration of drug action. At the same time, the introduction of tritium substituted phenyl groups may also affect the solubility and permeability of drug molecules, improve the bioavailability of drugs, and enable drugs to better exert therapeutic effects. So it may be applied in multiple fields of drug development. For example, in the development of anti-tumor drugs, it can serve as an intermediate for synthesizing compounds with anti-tumor activity; In the development of antibacterial drugs, it can be used to synthesize compounds with antibacterial activity; In addition, it may also be used to synthesize drug molecules with other biological activities such as anti-inflammatory and antioxidant properties.

In Chemical Experiments

 

This compound can be used as an analytical standard in experiments such as chromatography and mass spectrometry analysis. Its stable chemical properties and clear chemical structure make it an ideal choice for qualitative and quantitative analysis. By comparing the chromatogram or mass spectrum of the test sample with the standard sample, it is possible to accurately determine whether the sample contains the target compound and the content of the target compound. It can also be used as an adsorption indicator or complexation indicator. In chemical analysis, indicators are used to indicate the endpoint of a chemical reaction or the presence of a certain component during the reaction process. Its unique chemical properties enable it to undergo color or fluorescence changes under specific conditions, indicating the progress or outcome of the reaction.

Other applications

 

Due to the tritium substitution of the benzene ring in it (i.e. some hydrogen atoms are replaced by deuterium atoms), it becomes an ideal choice for isotope labeling analysis. Isotope labeling analysis is a method of using radioactive or non radioactive isotope labeled compounds to track their behavior in living organisms or chemical reactions. By introducing tritium substituted phenyl, the position, conversion pathway, and interactions with other molecules of the compound in the reaction system can be traced. In addition, it may also have potential application value in chemical fields such as rubber and dyes.

9-Bromo-10-(phenyl-d5)anthracene, also known by its CAS number 1185864-38-3, is a deuterated derivative of 9-bromo-10-phenylanthracene. This compound has garnered interest in the scientific community due to its potential applications in fields such as organic electronics, pharmaceuticals, and materials science.

The research began with the exploration of its parent compound, 9-bromo-10-phenylanthracene. This compound is a well-known organic synthetic intermediate, valued for its unique multi-aromatic ring structure. Its synthesis and properties have been extensively studied, paving the way for the development of deuterated variants like 9-bromo-10-(phenyl-d5)anthracene.

Deuteration, the process of replacing hydrogen atoms with deuterium (an isotope of hydrogen), is often employed to enhance the properties of organic molecules. Deuteration is believed to improve its stability and performance in applications such as organic light-emitting diodes (OLEDs). The "heavy atom effect" introduced by deuterium can enhance the spin-orbit coupling, leading to improved phosphorescence and quantum efficiency.

The synthesis typically involves the use of deuterated starting materials or deuterium-labeled reagents. One common method involves the Suzuki coupling reaction between 9,10-dibromoanthracene and deuterated phenylboronic acid. This approach allows for the selective introduction of deuterium atoms into the phenyl ring, resulting in the desired deuterated product.

Over the years, researchers have focused on optimizing the synthesis conditions to improve yield and purity. They have also explored the use of different catalysts and solvents to enhance the efficiency of the reaction. These efforts have led to the development of more reliable and scalable synthesis routes.

In addition to its synthetic development, it has been studied for its optical and electronic properties. Its unique molecular structure makes it an attractive candidate for use in OLEDs and other optoelectronic devices. Researchers have investigated its photoluminescence, electroluminescence, and charge transport properties, seeking to understand how deuteration affects these characteristics.

As research continues, its potential applications in various fields are being explored. Its stability, enhanced optical properties, and compatibility with other materials make it a promising candidate for use in advanced materials and devices. Future research is likely to focus on further optimizing its synthesis and exploring new applications for this fascinating compound.

Hot Tags: 9-bromo-10-(phenyl-d5)anthracene cas 1185864-38-3, suppliers, manufacturers, factory, wholesale, buy, price, bulk, for sale, 4 4 5 5 tetramethyl 2 triphenylen 2 yl 1 3 2 dioxaborolane, 3 6 Di tert butylfluorenone, Benz b indolo 2 3 d 1 benzazepine 5 10 dihydro 5 phenyl , 4 4 naphthalene 1 2 diylbis 4 1 phenylene bis 2 phenylbenzo h quinazoline , 9 9 Bis 1 1 biphenyl 3 yl 3 3 bi 9H carbazole, CAS 1898210 08 6